Evidence map›Paper›PMID 37077930›Full record

ReviewThe Journal of clinical and aesthetic dermatology2023

A Physician's Guide to the Use of Gene Expression Profile Ancillary Diagnostic Testing for Cutaneous Melanocytic Neoplasms.

Etan Marks, Abel Jarell, Joanna Ludzik, Aaron S Farberg, Harold S Rabinovitz, Robert G Phelps, Clay J Cockerell, Alexander Witkowski

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of clinical and aesthetic dermatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 8 institutions in 2 countries.

Etan MarksDr. Marks is with Dermatopathology, Kansas City University-Graduate Medical Education Consortium in Oviedo, Florida, and Advanced Dermatology and Cosmetic Surgery in Oviedo, Florida.
Abel JarellDr. Jarell is with Granite State Dermatology, PC in Portsmouth, New Hampshire.
Joanna LudzikDrs. Ludzik and Witkowski are with the Department of Dermatology, Oregon Health & Science University in Portland, Oregon.
Aaron S FarbergDr. Farberg is with Baylor Scott & White Health System in Dallas, Texas.
Harold S RabinovitzDr. Rabinovitz is with the Department of Dermatology, Medical College of Georgia in Augusta, Georgia.
Robert G PhelpsDr. Phelps is with Mount Sinai Hospital in New York City, New York.
Clay J CockerellDr. Cockerell is with Cockerell Dermatopathology in Dallas, Texas and the Departments of Dermatology and Pathology, UT Southwestern Medical Center in Dallas, Texas.
Alexander WitkowskiDrs. Ludzik and Witkowski are with the Department of Dermatology, Oregon Health & Science University in Portland, Oregon.
Advanced Dermatology · USAugusta University · USBaylor Scott & White Health · USGranite State College · USJagiellonian University · PLMount Sinai Hospital · USOregon Health & Science University · USSouthwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Some melanocytic neoplasms suspicious for melanoma require additional workup to arrive at a final diagnosis. Within the last eight years, gene expression profiling (GEP) has become an important ancillary tool to aid in the diagnosis of melanocytic neoplasms with uncertain malignant potential. As the usage of two commercially available tests (23-GEP and 35-GEP) evolves, it is important to answer key questions about optimal utilization and their impact on patient care. Methods: Recent and relevant articles answering the following questions were included in the review. First, how do dermatopathologists synthesize the available literature, the latest guidelines, and their clinical experience to determine which cases would be most likely to benefit from GEP testing? Second, how best can a dermatologist convey to their dermatopathologist that the use of GEP in the diagnostic process could provide a more clearly defined result and thereby help empower the dermatologist to provide higher-quality patient care when making specific patient management decisions for otherwise pathologically ambiguous lesions? Results: When interpreted in the context of the clinical, pathologic, and laboratory information, GEP results can facilitate the rendering of timely, accurate, and definitive diagnoses for melanocytic lesions with otherwise uncertain malignant potential to inform personalized treatment and management plans. Limitations: This was a narrative review focused on clinical use of GEP compared to other ancillary diagnostic tests performed postbiopsy. Conclusion: Open communication between dermatopathologists and dermatologists, especially regarding GEP testing, can be a vital component to achieve appropriate clinicopathologic correlation for otherwise ambiguous melanocytic lesions.

Indexed as

23-GEP35-GEPancillary diagnostic testingconfocalcutaneous melanomadermoscopydiagnosisgene expression profileGEPhistopathologymelanocytic lesionsmelanoma

Identifiers

PMID37077930
PMCPMC10110288
OpenAlexW4366602311

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.